Calculate the incidence of eclampsia; cardiac arrest and perimortem caesarean sectio in pregnancy or puerperium in the Netherlands.
ID
Bron
Verkorte titel
Aandoening
Eclampsia; Cardiac Arrest; Perimortem caesarean section; maternal morbidity; maternal mortality; INOSS; NethOSS; LEMMoN
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Incidence
All variables will be ascertained from anonymised photocopies from case-files and entered in a secured database.
Incidence will be calculated using the CBS data on deliveries per anum.
Achtergrond van het onderzoek
The NethOSS is a national registration network of severe maternal morbidity. It uses a monthly mailing card to identify cases of specific form of morbidity to ascertain incidence, putative risc factors and managemengt strategies by retriewing this data from anonymised photocopies of case files.
Doel van het onderzoek
Calculate the incidence of eclampsia; cardiac arrest and perimortem caesarean sectio in pregnancy or puerperium in the Netherlands.
Onderzoeksproduct en/of interventie
none. Since this is an national observational study, there are no interventions applicable.
Algemeen / deelnemers
[default]
The Netherlands
Wetenschappers
[default]
The Netherlands
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Eclampsia:
Any woman with convulsion(s) during pregnancy or in the first 10 days postpartum, not attributable to other causes.
Cardiac arrest:
Any pregnant women in the Netherlands identified as receiving basic life support (chest compressions and, where possible, ventilation breaths), including women who have undergone PMCS.
Amniotic fluid embolism:
IN THE ABSENCE OF ANY OTHER CLEAR CAUSE
Either:
Acute maternal collapse with one or more of the following features:
• Acute fetal compromise
• Cardiac arrest
• Cardiac rhythm problems
• Coagulopathy
• Hypotension
• Maternal hemorrhage*
• Premonitory symptoms (restlessness, numbness, agitation, tingling)
• Seizure
• Shortness of breath
* Excluding women with maternal haemorrhage as the first presenting feature in whom there was no evidence of early coagulopathy or cardio-respiratory compromise
Or
Women in whom the diagnosis was made at post-mortem examination with the finding of fetal squames or hair in the lungs
Control group:
For every case of eclampsia, a matching control will be retriewed from the reporting hospital. Controls will be retriewed by using the hospital registrtion of deliveries. Controls a matched only of parity.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Not meeting inclusion criteria.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL3988 |
NTR-old | NTR4160 |
Ander register | METC LUMC : P12.216/SH/sh |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |